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通过接种非活性细菌刺激保护性CD8 + T淋巴细胞。

Stimulation of protective CD8+ T lymphocytes by vaccination with nonliving bacteria.

作者信息

Szalay G, Ladel C H, Kaufmann S H

机构信息

Department of Immunology, University of Ulm, Germany.

出版信息

Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12389-92. doi: 10.1073/pnas.92.26.12389.

Abstract

Infectious diseases caused by intracellular microbes are responsible for major health problems, and satisfactory control will ultimately depend on efficient vaccination strategies. The general assumption is that activation of protective immune responses against intracellular microbes dominated by CD8+ T cells are achieved only by live vaccines. In contrast, we here demonstrate stimulation of protective immunity in mice against the intracellular pathogen Listeria monocytogenes by vaccination with heat-killed listeriae. Vaccine-induced immunity comprised cytolytic and interferon gamma-producing CD8+ T lymphocytes. CD8+ T cells from vaccinated donor mice transferred protection against listeriosis. Moreover, vaccination with heat-killed listeriae induced production in CD4+ T-cell-deficient, H2-A beta gene-disrupted mutant mice. We conclude that antigens from killed listeriae are introduced into the major histocompatibility complex class I pathway and thus are recognized by CD8+ T cells. The practicability of killed vaccines against human infectious diseases therefore should be reevaluated.

摘要

由细胞内微生物引起的传染病是主要的健康问题,而令人满意的控制最终将取决于有效的疫苗接种策略。一般的假设是,针对以CD8 + T细胞为主导的细胞内微生物的保护性免疫反应的激活仅通过活疫苗来实现。相比之下,我们在此证明,通过用热灭活的李斯特菌进行疫苗接种,可刺激小鼠针对细胞内病原体单核细胞增生李斯特菌产生保护性免疫。疫苗诱导的免疫包括细胞溶解和产生干扰素γ的CD8 + T淋巴细胞。来自接种疫苗的供体小鼠的CD8 + T细胞可传递针对李斯特菌病的保护作用。此外,用热灭活的李斯特菌进行疫苗接种可在CD4 + T细胞缺陷、H2 - Aβ基因破坏的突变小鼠中诱导产生。我们得出结论,来自灭活李斯特菌的抗原被引入主要组织相容性复合体I类途径,因此被CD8 + T细胞识别。因此,应重新评估灭活疫苗针对人类传染病的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0113/40363/d5ab609bc737/pnas01504-0454-a.jpg

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